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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050773Generated: October 31, 2026

2-Methyl-4-methoxypyridine-N-oxide → (4-methoxypyridin-2-yl)methyl Acetate

https://huagongshe.com/reaction/2050773

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-4-methoxypyridine-N-oxideHCID 10701893—
Reactant2-Acetoxymethyl-6-chloropyridineHCID 10726190—
Product(4-methoxypyridin-2-yl)methyl AcetateHCID 10726082—

Reaction Steps

Starting with 2-methyl-4-methoxypyridine-1-oxide (2.1 g) in the procedure of Part (ii) afforded 2.5 g of 2-acetoxymethyl-4-methoxypyridine which was contaminated with about 25% of 5-acetoxy-2-methyl-4-methoxypyridine. This mixture was dissolved in methanol (10 ml) containing 1.118 g (20.7 mmole) sodium methoxide and stirred at reflux for one hour. The methanol was evaporated in vacuo, the residue diluted with water, neutralized with dilute hydrochloric acid and extracted with chloroform. The organic layer was washed with brine, dried (MgSO4) and concentrated in vacuo to give 853 mg (41%) 2-hydroxymethyl-4-methoxypyridine. 1H-NMR(CDCl3)ppm (delta): 3.9 (s, 3H), 4.72 (s, 2H), 5.35 (bs, 1H), 6.7 (dd, 1H), 6.95 (d, 1H), 8.3 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05015473
Source datasetuspto-grants-1991_05
ORD IDord-4df8e2fc6e9148b58a384d43c71a5c6e
Source noteuspto-grants-1991_05